A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3531198



Internal ID18829479
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:74104530..74133231hg38UCSC Ensembl
Innerchr14:74571233..74599934hg19UCSC Ensembl
Innerchr14:73640986..73669687hg18UCSC Ensembl
Cytoband14q24.3
Allele length
AssemblyAllele length
hg3828702
hg1928702
hg1828702
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1039710
Supporting Variants
Samples
Known GenesLIN52
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3531198
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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